Skip to content

Data Collection Using Healthtech (Binah.ai) Application

Vital Signs Data Collection Using Binah.ai Application - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/06/053570
Enrollment
300
Registered
2023-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Binah.ai Ltd.
Lead Sponsor
Nuverse Health Solutions Pvt Ltd
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subject must have the ability to understand and provide written informed consent.2. Male or female subject more than or equal to 18 and less than or equal to 65 years of age;3. Subject must be willing and able to comply with study procedures.4.In addition to the above criteria, the target population should include adult subjects with at least one of the following: •Diabetes or pre-diabetes HbA1C 5.7-13% (both inclusive) •Hypertension with systolic measurements above 130 mmHg •Total cholesterol above 200 mg/dl and/or LDL above 130 mg/dl •Atrial fibrillation•Smokers approximately 20-30% of all subjects

Exclusion criteria

Exclusion criteria: 1. Subject with compromised circulation, injury, or physical malformation of fingers, hands, ears or forehead/skull or other sensor Region of Interest (ROI) which would limit the ability to test ROI needed for the study. Note: Certain malformations may still allow subjects to participate if the condition is noted and would not affect the particular areas utilized. 2. Subject has a tattoo in the optical path which would limit the ability to test ROI needed for the study. 3. Subjects with severe contact allergies to standard adhesives, latex or other materials found in pulse oximetry sensors, respiration monitor electrodes or other medical sensors used for measuring vital signs. 4. Subject with a medical condition which in the opinion of the investigator, does not allow performing the study assessments. 5. Subject unfit to participate in the study to the judgment of the investigator.

Design outcomes

Primary

MeasureTime frame
1.Oxygen saturation, pulse rate, respiratory rate, & blood pressure (systolic & diastolic) data collection using the Binah.ai application & reference devices 2.Estimation through blood sample (Complete Blood Count ,HbA1C, Lipid Profile ,Cotinine, Glucose, Albumin, Globulin, Neutrophils, Lymphocytes, Creatinine, Urea, Sodium, Kalium, Calcium, hsCRP & Magnesium.)Timepoint: Single day study

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactKfir Oved

Binah.ai

naveh.tov@binah.ai52-9635688

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026